Just 1 test to diagnose AML?!!

Research output: Contribution to journalComment/debatepeer-review

Abstract

In this issue of Blood, McKerrell et al describe a novel next-generation sequencing (NGS)-based platform for the identification of point mutations, common fusion genes, and copy-number alterations in acute myeloid leukemia (AML) and myelodysplastic syndromes (MDS) from a single genomic DNA sample.

Original languageEnglish
Pages (from-to)7-8
Number of pages2
JournalBlood
Volume128
Issue number1
DOIs
Publication statusPublished - 7 Jul 2016

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